FIELD: organic chemistry, biochemistry, pharmacy. SUBSTANCE: invention relates to condensed pyridazine of the general formula (I) where n = 1 or 2; R1- - hydrogen, halogen atom, nitro-, cyano-, amino-group or 4-hydroxypiperidine-1-yl; R2 and R3- - halogen atom or lower alkoxy-group, or R2 and R3 form together methylenedihydroxy- -group; symbol _ _ _ means double or simple bond; when _ _ _ is a double bond then X - nitrogen atom and Y means =C-Z where Z - halogen atom, group of the formulas (a), (b), (c), (d), (e), (f); p = 0 or 1; m = 0, 1, 2; R4 means carbamoyl-, carboxy-, carboxylate-group with cation, alkoxycarbonyl- or dialkylamino-group; R5 or R6 means H and other - hydroxyl; R7 means pyridyl, pyrimidyl or lower hydroxyalkyl; R8- means H, lower alkyl; R9- means pyridyl, lower hydroxyalkyl, carboxyalkyl, lower alkoxy-, lower hydroxyalkoxy-group, hydroxymethylpyrrolidinyl, imidazolyl, morpholinyl, pyridylmethyl; when _ _ _ means a simple bond then X means NR10 where R10 means H, carboxymethyl, lower alkoxycarbonylmethyl, tetrahydropyranylalkyl or hydroxyalkyl; Y means carbonyl. Synthesized compounds show inhibitory activity with respect to cyclic GMP-phosphodiesterase. EFFECT: improved method of synthesis. 13 cl, 1 tbl, 73 ex
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Authors
Dates
1999-03-27—Published
1995-08-08—Filed